Zobrazeno 1 - 10
of 446
pro vyhledávání: '"Lisa J, Martin"'
Autor:
Brian A. Upton, Kristen N. Krolick, Xue Zhang, Valentina Pilipenko, Lisa J. Martin, Hong Ji, Susan Glynn, Kristi Barnett, Arjunan Ganesh, Constance L. Monitto, Lisa M. Einhorn, Radhamangalam J. Ramamurthi, Vidya Chidambaran
Publikováno v:
PAIN Reports, Vol 9, p e1201 (2024)
Abstract. Introduction:. Mu opioid receptor gene (OPRM1) variant rs1799971 introduces a CpG site, which may influence DNA methylation (DNAm) and opioid/pain outcomes. Objectives:. In this nested analysis, we investigated both OPRM1 A118G genotype and
Externí odkaz:
https://doaj.org/article/14cf3a1857584b93a1f5734ee3ba2d49
Autor:
Donna Langley, Pawel Sadowski, Zoe Dettrick, Giorgio Stefanutti, Roy Kimble, Craig Munns, Tuo Zang, Andrew J.A. Holland, Mark W. Fear, Lisa J. Martin, Fiona M. Wood, Leila Cuttle
Publikováno v:
Burns Open, Vol 8, Iss 2, Pp 147-156 (2024)
The most recognised role of vitamin D in the body is for calcium absorption, and sufficiency is defined as a vitamin D blood serum level greater than 20 ng/mL (50 nmol/L). In growing children, hypovitaminosis D is associated with bone and muscle weak
Externí odkaz:
https://doaj.org/article/1121d4ec99354460a579101344d8b56f
Autor:
Stanley B. DeVore, Matthew Schuetz, Lauren Alvey, Henry Lujan, David E. Ochayon, Lindsey Williams, Wan Chi Chang, Alyssa Filuta, Brandy Ruff, Arjun Kothari, Jennifer M. Hahn, Eric Brandt, Latha Satish, Krishna Roskin, Andrew B. Herr, Jocelyn M. Biagini, Lisa J. Martin, Deniz Cagdas, Sevgi Keles, Joshua D. Milner, Dorothy M. Supp, Gurjit K. Khurana Hershey
Publikováno v:
Cell Reports, Vol 43, Iss 8, Pp 114589- (2024)
Summary: Caspase recruitment domain family member 14 (CARD14) and its variants are associated with both atopic dermatitis (AD) and psoriasis, but their mechanistic impact on skin barrier homeostasis is largely unknown. CARD14 is known to signal via N
Externí odkaz:
https://doaj.org/article/93643c0fb9c04c9683a5cbbebc4dcd2e
Publikováno v:
HGG Advances, Vol 5, Iss 3, Pp 100286- (2024)
Summary: Genetic testing with exome sequencing and genome sequencing is increasingly offered to infants and children with cardiovascular diseases. However, the rates of positive diagnoses after genetic testing within the different categories of cardi
Externí odkaz:
https://doaj.org/article/6c06b15aec4143bfb132259c13f4e3e8
Publikováno v:
European Burn Journal, Vol 5, Iss 2, Pp 77-89 (2024)
Parents’ emotions after their child’s burn might be influenced by the injury circumstances or demographic characteristics of the patient and family. Parents’ post-traumatic stress symptoms and their child’s distress may interact and affect em
Externí odkaz:
https://doaj.org/article/0d840c074e0247a1bbf800f7c0dcedfc
Autor:
Brad G. Kurowski, Amery Treble-Barna, Valentina Pilipenko, Lisa J. Martin, Anil G. Jegga, Aimee E. Miley, Nanhua Zhang, Anthony Fabio, Ranjit S. Chima, Anna-Lynne R. Adlam, Kenneth Kaufman, Michael J. Bell, Sue R. Beers, Stephen R. Wisniewski, Shari L. Wade, TBI Genetics and Environment Study Team
Publikováno v:
Frontiers in Systems Biology, Vol 4 (2024)
Introduction: There is significant unexplained variability in behavioral and executive functioning after pediatric traumatic brain injury (TBI). Prior research indicates that there are likely genetic contributions; however, current research is limite
Externí odkaz:
https://doaj.org/article/ef70d6c38f6e4c31b24d60c6d0614514
Autor:
Guillermo Torres, Andrew C. Lancaster, Jun Yang, Megan Griffiths, Stephanie Brandal, Rachel Damico, Dhananjay Vaidya, Catherine E. Simpson, Lisa J. Martin, Michael W. Pauciulo, William C. Nichols, David D. Ivy, Eric D. Austin, Paul M. Hassoun, Allen D. Everett
Publikováno v:
Pulmonary Circulation, Vol 13, Iss 3, Pp n/a-n/a (2023)
Abstract Insulin‐like growth factor (IGF) binding proteins (IGFBPs) are a family of growth factor modifiers, some of which are known to be independently associated with pulmonary arterial hypertension (PAH) survival. IGF factor binding protein 7 (I
Externí odkaz:
https://doaj.org/article/9d104d23bbbd4d9993ff27a2919093a7
Autor:
Andrea Edwards, Ashley Teusink‐Cross, Lisa J. Martin, Cynthia A. Prows, Parinda A. Mehta, Laura B. Ramsey
Publikováno v:
Clinical and Translational Science, Vol 15, Iss 3, Pp 610-618 (2022)
Abstract Chemotherapy‐induced nausea and vomiting (CINV) is commonly experienced by patients receiving antineoplastic agents prior to hemopoietic stem cell transplant (HSCT). Ondansetron, a 5‐HT3 antagonist metabolized by CYP2D6, is an antiemetic
Externí odkaz:
https://doaj.org/article/049767258135467290e37ec23abfcaba
Publikováno v:
Clinical and Translational Science, Vol 15, Iss 1, Pp 63-69 (2022)
Abstract Low‐dose methotrexate (MTX) is an immunosuppressant used to treat inflammatory bowel disease (IBD). SLCO1B1 genetic variation has been associated with delayed MTX clearance and increased toxicity. The purpose of this study was to evaluate
Externí odkaz:
https://doaj.org/article/7312e4e443344c46acccaabfd37284d5
Autor:
Tetsuo Shoda, Kenneth M. Kaufman, Ting Wen, Julie M. Caldwell, Garrett A. Osswald, Pathre Purnima, Nives Zimmermann, Margaret H. Collins, Kira Rehn, Heather Foote, Michael D. Eby, Wenying Zhang, Netali Ben-Baruch Morgenstern, Adina Y. Ballaban, Jeff E. Habel, Leah C. Kottyan, J. Pablo Abonia, Vincent A. Mukkada, Philip E. Putnam, Lisa J. Martin, Marc E. Rothenberg
Publikováno v:
Nature Communications, Vol 12, Iss 1, Pp 1-15 (2021)
Eosinophilic esophagitis (EoE) is a chronic allergic inflammatory disease with a complex underlying genetic etiology. Here, the authors identify a series of rare variants in DSP and PPL in multiplex families with EoE and uncover a pathogenic role for
Externí odkaz:
https://doaj.org/article/f2e541c35dcb4834913ac2dfae852b00